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Congenital sialidosis type 2
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Juvenile sialidosis type 2
Sialidosis type 1
Galactosialidosis
GM1 gangliosidosis type 1
GM1 gangliosidosis type 2
GM1 gangliosidosis type 3
Mucopolysaccharidosis type 4B
LIG4 syndrome
Omenn syndrome
Mucopolysaccharidosis type 4A
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
NEU1 Q99519608272
No signs/symptoms info available.